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Applied Pharmacokinetics in the Adult Critically Ill Gil Fraser, PharmD, FCCM Critical Care Tom Nolin, PharmD, PhD Nephrology and Transplantation Maine Medical Center Portland, ME
Why Study Pharmacokinetics?   ,[object Object],[object Object],[object Object],[object Object],[object Object]
Pharmacokinetics ,[object Object],[object Object],[object Object],[object Object]
Drug Absorption Occurs Via Many Routes of Administration ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],* This discussion pertains to enteral drug absorption
Enteral Drug Absorption ,[object Object],[object Object],[object Object],[object Object],[object Object]
Sites of pre-systemic metabolism via CYP 3A and efflux by P-glycoprotein GI drug absorption and pre-systemic metabolism
Oral/Enteral Drug Administration ,[object Object],[object Object],[object Object],[object Object],[object Object]
Oral/Enteral Drug Administration Should Be Avoided in Those With… ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Interacting GI Substances May Interfere with Absorption ,[object Object],[object Object],[object Object],[object Object],[object Object]
Distribution ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Central Nervous System Effects of Medications and the Blood-brain Barrier ,[object Object],[object Object]
Why Does Midazolam Change From a Short- to a Long-acting Benzodiazepine When Given for a Prolonged Period of Time? Hours Duration of midazolam therapy Chest. 1993;103:55.
Context Specific Half-life Accumulation in a deep compartment is a function of fat solubility and may explain the long duration of action of midazolam after long-term use.
How can the volume of distribution help predict removal by hemodialysis? How about the extent of protein binding? If a drug has a large volume of distribution, very little resides in the circulation and is available for removal via hemodialysis.  Examples  -  digoxin and tricyclic antidepressants Highly protein bound drugs are typically not removed by hemodialysis.
The Clinical Relevance of Deranged Protein Binding of Drugs Has Been Overstated (Except for Phenytoin) ,[object Object],[object Object],[object Object],[object Object],Clin Pharmacol Ther. 2002;71:115.
P-glycoprotein  (P-gp) and Drug  Distribution   ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
The transmembrane protein  P-glycoprotein   is believed to function as an energy-dependent efflux pump or drug transporter.  P-gp Inhibitors: Verapamil Grapefruit juice Amiodarone Quininidine Clarithromycin Tariquidar P-gp Inducers: Rifampin St. John’s Wort
Drug Metabolism ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Consequences of Drug Metabolism Substrate (drug) Enzyme Metabolite Active Inactive Inactive Active Toxic Nontoxic Nontoxic Toxic Detoxification Prodrug Reactive metabolite Activation
Phases of Drug Metabolism Phase I ,[object Object],[object Object],[object Object],[object Object],[object Object]
[object Object],[object Object],[object Object],[object Object],[object Object],Phases of Drug Metabolism Phase II
Phases of Drug Metabolism Phase I Phase II benzene phenol phenyl sulfate Increasing polarity of drug/metabolite
Drug Metabolism ,[object Object],[object Object],[object Object]
Cytochrome P450 ,[object Object],[object Object],[object Object],[object Object],[object Object]
Contribution of CYP to Drug Metabolism Adapted from Clin Pharmacokinet 1997;32:210.
3A4/5 30% 1A2 13% 2E1 7% 2D6 4% 2C8 < 1% 2B6 < 1% 2A6 4% 2C19 2% 2C9 18% Nicotine Buproprion Mephenytoin Omeprazole Diazepam Coumarin Losartan NSAIDs Warfarin Tolbutamide Phenytoin Midazolam CyA/Tacrolimus CCBs Statins Cisapride Terfenadine Caffeine Theophyline Imipramine Chlorzoxazone Acetaminophen Nitrosamines Anesthetics Azoles Macrolides Cimetidine Grapefruit Barbs Rifampin Dexamethasone Carbamazepine St. John’s Wort Azoles Macrolides Cimetidine Grapefruit CYP450 Substrates SSRIs Desipramine Nortriptyline ß-blockers Debrisoquine D-methorphan Retinoids Paclitaxel Inhibitors Disulfiram Quinidine Methadone Cimetidine Azoles Azoles Inducers Barbs Rifampin Barbs Rifampin Omeprazole Barbs Rifampin PAHs Ethanol Isoniazid Benzene Rifampin
Drug Metabolism Often Results in Active Metabolites that Can Accumulate (Especially in Renal Disease) ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Drug Excretion ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Estimating Renal Function Using Serum Creatinine ,[object Object],[object Object],[object Object],[object Object]
Problem Drugs in Renal Disease ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Pharmacokinetic Principles ,[object Object],[object Object],[object Object],[object Object]
Half-life ,[object Object],[object Object]
Loading Doses ,[object Object],[object Object],[object Object]
 
Linear Kinetics ,[object Object],[object Object],[object Object]
Non-linear Kinetics ,[object Object],[object Object],[object Object],[object Object]
Steady-state plasma concentration Effect of increasing daily dose on steady-state drug concentrations for drugs undergoing nonlinear (  ) and linear (  ) kinetics Daily Dose Enzyme saturation for nonlinear drug
Contribution of Pharmagenetics to Interindividual Variability in Drug Response ,[object Object]
Clinical Relevance ,[object Object],[object Object],[object Object]
Pharmacogenetics The study of heredity as it relates to the absorption, distribution, elimination, and action of medicines A tool to limit variability and individualize therapy
Pharmacogenetics N Engl J Med. 2003;348:529.
Clinical Consequences of Genetic Polymorphisms ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Drug: Gene Interaction ,[object Object],[object Object],Do allelic variants of drug metabolizing enzymes impact pharmacokinetics and response?
Relationship between CYP2D6 genetic status and nortriptyline pharmacokinetics Clin Pharmacol Ther. 1998;63:444. TIPS. 1999;20:342.
Utility of Pharmacogenetics Ann Rev Genomics Hum Genet. 2001;2:9.
Summary: Management of Drug Therapy Using  PK Principles ,[object Object],[object Object],[object Object],[object Object],[object Object],[object Object],[object Object]
Selected References ,[object Object],[object Object],[object Object],[object Object]
Case Scenario #1   ,[object Object],[object Object],[object Object],[object Object],[object Object]
Case Scenario #1 - Answer ,[object Object],[object Object],[object Object]
Case Scenario #2 ,[object Object],[object Object],[object Object],[object Object]
Case Scenario #2 - Answer ,[object Object],[object Object],[object Object],[object Object]
Case Scenario #3 ,[object Object],[object Object],[object Object],[object Object]
Case Scenario #3 - Answer ,[object Object],[object Object],[object Object]

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Pharmacokinetics

  • 1. Applied Pharmacokinetics in the Adult Critically Ill Gil Fraser, PharmD, FCCM Critical Care Tom Nolin, PharmD, PhD Nephrology and Transplantation Maine Medical Center Portland, ME
  • 2.
  • 3.
  • 4.
  • 5.
  • 6. Sites of pre-systemic metabolism via CYP 3A and efflux by P-glycoprotein GI drug absorption and pre-systemic metabolism
  • 7.
  • 8.
  • 9.
  • 10.
  • 11.
  • 12. Why Does Midazolam Change From a Short- to a Long-acting Benzodiazepine When Given for a Prolonged Period of Time? Hours Duration of midazolam therapy Chest. 1993;103:55.
  • 13. Context Specific Half-life Accumulation in a deep compartment is a function of fat solubility and may explain the long duration of action of midazolam after long-term use.
  • 14. How can the volume of distribution help predict removal by hemodialysis? How about the extent of protein binding? If a drug has a large volume of distribution, very little resides in the circulation and is available for removal via hemodialysis. Examples - digoxin and tricyclic antidepressants Highly protein bound drugs are typically not removed by hemodialysis.
  • 15.
  • 16.
  • 17. The transmembrane protein P-glycoprotein is believed to function as an energy-dependent efflux pump or drug transporter. P-gp Inhibitors: Verapamil Grapefruit juice Amiodarone Quininidine Clarithromycin Tariquidar P-gp Inducers: Rifampin St. John’s Wort
  • 18.
  • 19. Consequences of Drug Metabolism Substrate (drug) Enzyme Metabolite Active Inactive Inactive Active Toxic Nontoxic Nontoxic Toxic Detoxification Prodrug Reactive metabolite Activation
  • 20.
  • 21.
  • 22. Phases of Drug Metabolism Phase I Phase II benzene phenol phenyl sulfate Increasing polarity of drug/metabolite
  • 23.
  • 24.
  • 25. Contribution of CYP to Drug Metabolism Adapted from Clin Pharmacokinet 1997;32:210.
  • 26. 3A4/5 30% 1A2 13% 2E1 7% 2D6 4% 2C8 < 1% 2B6 < 1% 2A6 4% 2C19 2% 2C9 18% Nicotine Buproprion Mephenytoin Omeprazole Diazepam Coumarin Losartan NSAIDs Warfarin Tolbutamide Phenytoin Midazolam CyA/Tacrolimus CCBs Statins Cisapride Terfenadine Caffeine Theophyline Imipramine Chlorzoxazone Acetaminophen Nitrosamines Anesthetics Azoles Macrolides Cimetidine Grapefruit Barbs Rifampin Dexamethasone Carbamazepine St. John’s Wort Azoles Macrolides Cimetidine Grapefruit CYP450 Substrates SSRIs Desipramine Nortriptyline ß-blockers Debrisoquine D-methorphan Retinoids Paclitaxel Inhibitors Disulfiram Quinidine Methadone Cimetidine Azoles Azoles Inducers Barbs Rifampin Barbs Rifampin Omeprazole Barbs Rifampin PAHs Ethanol Isoniazid Benzene Rifampin
  • 27.
  • 28.
  • 29.
  • 30.
  • 31.
  • 32.
  • 33.
  • 34.  
  • 35.
  • 36.
  • 37. Steady-state plasma concentration Effect of increasing daily dose on steady-state drug concentrations for drugs undergoing nonlinear ( ) and linear ( ) kinetics Daily Dose Enzyme saturation for nonlinear drug
  • 38.
  • 39.
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